Medline MDR107002LRecalls & reported problems
Medline Industries, Inc. · BED, SEMI ELECTRIC, MEDLITE · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 31
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 31 adverse event reports that list this exact device (DI 40080196294320), received between May 6, 2026 and Sep 30, 2026 — classified as 31 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (16 reports).
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Recalls naming this device
- Nov 26, 2025Open, Classified
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
Z-1012-2026 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Electrical /Electronic Property Problem16
- Fracture4
- Mechanical Problem4
- Loose or Intermittent Connection2
- Complete Loss of Power1
- Crack1
- Insufficient Device Problem Information1
- Key or Button Unresponsive/not Working1
Patient problems
- No Clinical Signs, Symptoms or Conditions31
Recent adverse event reports
The 25 most recent of 31 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50948668 ↗MalfunctionSep 30, 2026Electrical /Electronic Property Problem
It was reported that "the pendant is not working and there is no function to the bed" and "wires are exposed on the pendant."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945341 ↗MalfunctionSep 29, 2026Fracture
It was reported that "Patient heard a pop noise when trying to raise head of bed, the motor snapped."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936930 ↗MalfunctionSep 29, 2026Crack
It was reported that "The frame of the bed has been cracked."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931460 ↗MalfunctionSep 28, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918632 ↗MalfunctionSep 28, 2026Fracture
It was reported that "this drivearm came apart during the bed test after it was cleaned. It doesn't want to go back together.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917349 ↗MalfunctionSep 24, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885239 ↗MalfunctionSep 23, 2026Electrical /Electronic Property Problem
It was reported that "for both beds all functions of the bed work besides the head/foot section of the bed will not go up or down." Customer stated that "the hand remote is not working and all they could hear is a \"humming or clicking noise\" and the bed does not move."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873235 ↗MalfunctionSep 23, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873177 ↗MalfunctionSep 23, 2026Material Frayed; Material Split, Cut or Torn
It was reported that "Bed remote and electrical cord got pinched in between bed. Both still work but there is tape over it."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50871512 ↗MalfunctionSep 22, 2026Fracture
It was reported that "The head shaft broke off that comes out of the actuator."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50857612 ↗MalfunctionSep 22, 2026Electrical /Electronic Property Problem
It was reported that Bed foot actuator quit working. It makes a noise but nothing happens.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855998 ↗MalfunctionSep 21, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50842956 ↗MalfunctionAug 24, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50418820 ↗MalfunctionAug 6, 2026Mechanical Problem
It was reported that foot spring would not raise. Took motor off and the bar that raises the foot section came loose from the motor.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50161339 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50007957 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50007705 ↗MalfunctionJul 27, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50002107 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50001608 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50001579 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50000819 ↗MalfunctionJul 27, 2026Key or Button Unresponsive/not Working
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50000812 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem; Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50000474 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50000116 ↗MalfunctionJul 27, 2026Electrical /Electronic Property Problem
It was reported that the foot spring does not respond at all.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50000045 ↗
Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices
- Centrella™ Bed P7900BHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL2 recalls5 deaths1,937 reports
- Progressa® Bed System P7500AHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death1,377 reports
- VersaCare® Med Surg Bed P3200KHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL3 deaths1,193 reports
- Medline MDR107002EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death374 reports
- Medline MDR107003EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall3 deaths362 reports
- InTouch 2141Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths361 reports
- Citadel Plus FX811B3B4AMABBArjohuntleigh AB · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths358 reports
- TotalCare® Bed P1900QHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL317 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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